Comparison of 6 SARS-CoV-2 Molecular Methods and Correlation With the Cycle Threshold Distribution in Clinical Specimens

Author:

Raju Saravanan1,Anderson Neil W1,Robinson Elizabeth2,Squires Crystal2,Wallace Meghan A1,Zhang Ray1,Burnham Carey-Ann D1345,Parikh Bijal A1

Affiliation:

1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA

2. Department of Laboratories, Barnes-Jewish Hospital, St. Louis, MO, USA

3. Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO, USA

4. Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA

5. Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA

Abstract

Abstract Background The detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in patient samples is of critical importance in the management of patients and monitoring transmission in the population. However, data on the analytical performance characteristics for detection of SARS-CoV-2 in clinical specimens between individual targets within the same platform, and among different analytical platforms, are limited. Methods Here we evaluated the performance of 6 different sample-to-answer SARS-CoV-2 detection methods—Roche cobas 6800, Cepheid GeneXpert, Diasorin Simplexa, Luminex Aries emergency use authorization (EUA), Luminex Aries research use only (RUO), and bioMérieux BioFire—in clinical specimens with a range of viral loads. Results The positive percentage agreement between the Roche cobas 6800 and GeneXpert was 100%, Diasorin 95%, Aries EUA 74%, Aries RUO 83%, and BioFire 97%. Notably, in samples with cycle threshold (Ct) values below 30 for the E gene on the Roche cobas 6800 platform, we found 100% positive agreement among all platforms. Given these results, we examined the distribution of over 10 000 Ct values of all positive specimens from individuals at our institution on the Roche cobas platform. Nearly 60% of specimens from asymptomatic individuals had a PCR Ct value >30 as measured using the cobas 6800 assay E gene. Conclusions Our results demonstrate performance characteristics between different platforms by Ct value and provide data regarding the distribution of viral RNA present in positive specimens.

Funder

Cepheid

bioMerieux

Luminex

BioFire

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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